Use of Perfusion Index Change as a Predictor of Hypotension During Propofol Sedation in Adult Patients Undergoing Hip Surgery Under Spinal Anesthesia: A Prospective Observational Study
NCT ID: NCT03556969
Last Updated: 2022-08-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
39 participants
OBSERVATIONAL
2018-05-21
2019-02-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Propofol sedation after SA
Participants who undergo propofol sedation after spinal anesthesia
Observation
no intervention
Interventions
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Observation
no intervention
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* pregnancy
* inability to measure noninvasive blood pressure on the arm
* preexisting hemodynamic instability
* known peripheral artery occlusive disease
* known autonomic nerve dysfunction
* uncontrolled hypertension
19 Years
ALL
No
Sponsors
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Samsung Medical Center
OTHER
Responsible Party
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Jong Hwan Lee
Associate Professor
Locations
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Samsung Medical Center, Sungkyunkwan University, School of Medicine
Seoul, , South Korea
Countries
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Other Identifiers
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2018-03-052
Identifier Type: -
Identifier Source: org_study_id
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